THERAFLOW SINGLE LUMEN AND THERAFLOW DUAL LUMEN— 510(k) K131023
Substantially EquivalentMedical Products, LLC
FDA 510(k) clearance K131023 for THERAFLOW SINGLE LUMEN AND THERAFLOW DUAL LUMEN, Substantially Equivalent on 2013-10-11. Applicant: Medical Products, LLC. Device class: 2.
Clearance details
- Applicant
- Medical Products, LLC
- Product code
- Code NFB
- Device class
- Class 2
- Regulation
- 21 CFR 868.5905
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Indianapolis, IN, US
Recent devices under product code NFB
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